FIELD OF THE INVENTION
[0001] This invention relates to stabilizing adjacent vertebrae of the spine by inserting
an intervertebral spacer, and more particularly an intervertebral spacer that is adjustable
in height, and a tool therefore.
BACKGROUND OF THE INVENTION
[0002] The vertebral or spinal column (spine, backbone) is a flexible assembly of vertebrae
stacked on top of each other extending from the skull to the pelvic bone which acts
to support the axial skeleton and to protect the spinal cord and nerves. The vertebrae
are anatomically organized into four generalized body regions identified as cervical,
thoracic, lumbar, and sacral; the cervical region including the top of the spine beginning
in the skull, the thoracic region spanning the torso, the lumbar region spanning the
lower back, and the sacral region including the base of the spine ending with connection
to the pelvic bone. With the exception of the first two cervical vertebrae, cushion-like
discs separate adjacent vertebrae, i.e. intervertebral discs.
[0003] The stability of the vertebral column during compression and movement is maintained
by the intervertebral discs. Each disc includes a gel-like center surrounded by a
fibrous ring. The gel-like center, i.e. nucleus pulposus, provides strength such that
the disc can absorb and distribute external loads and contains a mixture of type II-collagen
dispersed in a proteoglycan matrix. The fibrous ring, or annulus fibrosus, provides
stability during motion and contains laminated rings of type-I collagen. Thus, the
annulus fibrosis and the nucleus pulposus are interdependent, as the annulus fibrosis
contains the nucleus pulposus in place and the nucleus pulposus aligns the annulus
fibrosus to accept and distribute external loads. The integrity of the composition
and structure of the intervertebral disc is necessary to maintain normal functioning
of the intervertebral disc.
[0004] Many factors can adversely alter the composition and structure of the intevertebral
disc, such as normal physiological aging, mechanical injury/trauma, and/or disease,
resulting in impairment or loss of disc function. For example, the content of proteoglycan
in the nucleus pulposus declines with age, thus, it follows that the ability of the
nucleus pulposus to absorb water concurrently declines. Therefore, in normal aging
the disc progressively dehydrates, resulting in a decrease in disc height and possible
de-lamination of the annulus fibrosus. Mechanical injury can tear the annulus fibrosis
allowing the gel-like material of the nucleus pulposus to extrude into the spinal
canal and compress neural elements. Growth of a spinal tumor can impinge upon the
vertebrae and/or disc potentially compressing nerves.
[0005] Bones of the spine, and bony structures, generally, are susceptible to a variety
of weaknesses that can affect their ability to provide support and structure. Weaknesses
in bony structures have numerous potential causes, including degenerative diseases,
tumors, fractures, and dislocations. Advances in medicine and engineering have provided
doctors with a plurality of devices and techniques for alleviating or curing these
weaknesses.
[0006] In some cases, the spinal column, in particular, requires additional support in order
to address such weaknesses. One technique for providing support is to insert a spacer
between adjacent vertebrae.
[0007] US20110319997 describes a device known in the art that corresponds to the preamble of claim 1.
SUMMARY OF THE INVENTION
[0008] According to the invention it is provided a spacer having the features of claim 1.
Further advantageous features of the invention are set forth in the dependent claims.
[0009] In accordance with an embodiment of the disclosure, a spacer for separating bones
of a joint comprises a frame; a carriage slideably moveable in relation to the frame,
and having at least one ramped surface; an actuating screw connected to the carriage
and supported by the frame, the actuating screw configured to cause the carriage to
slideably move in relation to the frame when the actuating screw is rotated; a first
endplate configured to engage a first bone of the joint, and having at least one ramped
surface mateable with the at least one carriage ramped surface, whereby when the carriage
is slideably moved by rotation of the actuating screw, the at least one endplate ramped
surface slides against the at least one carriage ramped surface to cause the first
endplate to move along an axis transverse to the longitudinal axis, to increase a
height of the spacer; and a second endplate configured to engage a second bone of
the joint.
[0010] In various embodiments thereof, the endplate is continuously curved along its length;
the actuating screw is secured to the carriage by a nut; and the nut and the carriage
form a mating, curved bearing surface therebetween. According to the invention the
spacer further includes a screw support connected to the frame and configured to rotatably
retain the actuating screw; the screw support forms a longitudinal axis, and the frame
forms a longitudinal axis, and the screw support is slideably connected to the frame
to enable changing an angular orientation between the actuating screw and the frame.
[0011] In other embodiments thereof, the screw support is slideably connected to the frame
by a flanged connection; the first endplate is connected to the frame by a slideable
flanged connection.
[0012] In another embodiment thereof, the spacer further includes a pin moveable within
a slot formed in the carriage; and a link pivotably mounted to the pin, and including
a threaded bore into which the actuating screw is threadably engageable to cause the
carriage to slideably move within the frame.
[0013] In yet further embodiments thereof, the first endplate is slideably retained in connection
with the frame by a flanged connection; the spacer further includes a screw support
pivotally connected to the frame and rotatably supporting the actuating screw; the
carriage includes at least two ramped surfaces, and the second endplate includes at
least one ramped surface mateable with at least one of the at least two ramped surfaces
of the carriage, whereby when the carriage is slideably moved by rotation of the actuating
screw, the at least one second endplate ramped surface slides against the at least
one additional carriage ramped surface to cause the second endplate to move along
an axis transverse to the longitudinal axis to increase a height of the spacer.
[0014] In other embodiments thereof, the first endplate is configured to abut the frame
as the first endplate is moved along an axis transverse to the longitudinal axis,
whereby the first endplate moves substantially only along an axis transverse to the
longitudinal axis; at least one of the first endplate and the frame includes at least
one aperture through which a fastener may pass to secure the spacer to a bone of the
joint; the spacer further includes a blocking mechanism to prevent backing out of
a fastener passed through the first endplate; the first endplate includes one or more
projections configured to engage bone of the joint when the implant is positioned
between bones of the joint.
[0015] In another embodiment of the disclosure, not forming part of the invention, a method
of separating bones of a joint comprises inserting a spacer between bones of the joint,
the spacer including a frame; a carriage slideably moveable in relation to the frame,
and having at least one ramped surface; an actuating screw connected to the carriage
and supported by the frame, the actuating screw configured to cause the carriage to
slideably move in relation to the frame when the actuating screw is rotated; a first
endplate configured to engage a first bone of the joint, and having at least one surface
mateable with the at least one carriage ramped surface, whereby when the carriage
is slideably moveable by rotation of the actuating screw, the at least one endplate
ramped surface slides against the at least one carriage ramped surface to cause the
first endplate to move along an axis transverse to the longitudinal axis, to increase
a height of the spacer; and a second endplate configured to engage a second bone of
the joint.
[0016] In a yet further embodiment of the disclosure, a spacer for separating bones of a
joint comprises a frame; a carriage slideably moveable in relation to the frame, and
having at least two ramped surfaces; a screw support moveably connected to the frame
to form a changeable angular orientation with respect to the frame; an actuating screw
supported by the screw support and connected to the carriage, the actuating screw
configured to cause the carriage to slideably move in relation to the frame when the
actuating screw is rotated; and first and second endplates each configured to engage
an opposing bone of the joint, each having at least one ramped surface mateable with
at least one of the at least two carriage ramped surfaces, whereby when the carriage
is slideably moved by rotation of the actuating screw, the at least one ramped surface
of each of the first and second endplates slides against the at least one carriage
ramped surface to cause the first and second endplates to move relatively apart along
an axis transverse to the longitudinal axis, to increase a height of the spacer.
[0017] In a further embodiment it is provided a spacer for separating bones of a joint,
the spacer comprising: a frame; a carriage slideably moveable in relation to the frame,
and having at least one ramped surface; an actuating screw connected to the carriage
and supported by the frame, the actuating screw configured to cause the carriage to
slideably move in relation to the frame when the actuating screw is rotated; a first
endplate configured to engage a first bone of the joint, and having at least one ramped
surface mateable with the at least one carriage ramped surface, whereby when the carriage
is slideably moved by rotation of the actuating screw, the at least one endplate ramped
surface slides against the at least one carriage ramped surface to cause the first
endplate to move along an axis transverse to the longitudinal axis, to increase a
height of the spacer; and a second endplate configured to engage a second bone of
the joint, wherein at least one of the first endplate and the frame includes at least
one aperture through which a fastener may pass to secure the spacer to a bone of the
joint.
[0018] In a version, the spacer further includes a blocking mechanism to prevent backing
out of a fastener passed through the first endplate.
[0019] In a version, the first endplate includes one or more projections configured to engage
bone of the joint when the implant is positioned between bones of the joint. In a
further aspect of the disclosure, not forming part of the invention, it is provided
a method of separating bones of a joint, comprising: inserting a spacer between bones
of the joint, the spacer including a frame; a carriage slideably moveable in relation
to the frame, and having at least one ramped surface; an actuating screw connected
to the carriage and supported by the frame, the actuating screw configured to cause
the carriage to slideably move in relation to the frame when the actuating screw is
rotated; a first endplate configured to engage a first bone of the joint, and having
at least one surface mateable with the at least one carriage ramped surface, whereby
when the carriage is slideably moveable by rotation of the actuating screw, the at
least one endplate ramped surface slides against the at least one carriage ramped
surface to cause the first endplate to move along an axis transverse to the longitudinal
axis, to increase a height of the spacer; and a second endplate configured to engage
a second bone of the joint.
[0020] In a further embodiment, it is provided a spacer for separating bones of a joint,
the spacer comprising: a frame; a carriage slideably moveable in relation to the frame,
and having at least two ramped surfaces; a screw support moveably connected to the
frame to form a changeable angular orientation with respect to the frame; an actuating
screw supported by the screw support and connected to the carriage, the actuating
screw configured to cause the carriage to slideably move in relation to the frame
when the actuating screw is rotated; and first and second endplates each configured
to engage an opposing bone of the joint, each having at least one ramped surface mateable
with at least one of the at least two carriage ramped surfaces, whereby when the carriage
is slideably moved by rotation of the actuating screw, the at least one ramped surface
of each of the first and second endplates slides against the at least one carriage
ramped surface to cause the first and second endplates to move relatively apart along
an axis transverse to the longitudinal axis, to increase a height of the spacer.
BRIEF DESCRIPTION OF THE DRAWINGS
[0021] A more complete understanding of the disclosure, and the attendant advantages and
features thereof, will be more readily understood by reference to the following detailed
description when considered in conjunction with the accompanying drawings, in which:
FIG. 1 is a perspective view of a spacer implant of the disclosure, with an articulating
screw support;
FIG. 2 depicts a cross section of the spacer of FIG. 1, taken through an actuating
screw of the spacer, with the screw support oriented longitudinally, as further illustrated
in FIGS. 4 and 5;
FIG. 3 depicts the cross section of FIG. 2, with the spacer expanded by a separation
of endplates;
FIG. 4 depicts the spacer of FIG. 3, taken along an orientation 90 degrees offset
from the orientation of the spacer of FIG. 3;
FIG. 5 depicts the spacer of FIG. 2, taken along an orientation 90 degrees offset
from the orientation of the spacer of FIG. 2;
FIG. 6 depicts a cross section through the spacer of FIG. 1;
FIG. 7 depicts the spacer of FIG. 6, the endplates relatively separated;
FIG. 8 depicts a cross section of an alternative spacer of the disclosure shown in
FIG. 14, the endplates separated by pushing a carriage, having a screw support aligned
with a longitudinal axis of the spacer;
FIG. 9 depicts the spacer of FIG. 8, the endplates separated;
FIG. 10 depicts the spacer of FIG. 8, taken along an orientation 90 degrees offset
from the orientation of the spacer of FIG. 8;
FIG. 11 depicts the spacer of FIG. 10, the endplates separated;
FIG. 12 depicts the spacer of FIG. 11, the screw support disposed at an angle with
respect to the frame;
FIG. 13 depicts the spacer of FIG. 10, the screw support disposed at an angle with
respect to the frame;
FIG. 14 is a perspective view of an alternative embodiment of a spacer of the disclosure,
including a carriage which is pushed to separate endplates, and an actuator screw
which is displaced within a screw support;
FIG. 15 depicts the spacer of FIG. 14, the endplates separated;
FIG. 16 is a perspective view of an alternative spacer embodiment of the disclosure,
not forming part of the invention, having a curved shape;
FIG. 17 depicts a cross section of the spacer of FIG. 16, the endplates not separated;
FIG. 18 depicts a cross section of the spacer of FIG. 16;
FIG. 19 is a perspective view of an alternative spacer embodiment of the disclosure,
not forming part of the invention, the actuating screw secured to the carriage by
a nut;
FIG. 20 depicts a top view of the spacer of FIG. 19; and
FIG. 21 is a cross section of the spacer of FIG. 19.
DETAILED DESCRIPTION OF THE INVENTION
[0022] As required, detailed embodiments are disclosed herein; however, it is to be understood
that the disclosed embodiments are merely examples and that the systems and methods
described below can be embodied in various forms. Therefore, specific structural and
functional details disclosed herein are not to be interpreted as limiting, but merely
as a basis for the claims and as a representative basis for teaching one skilled in
the art to variously employ the present subject matter in virtually any appropriately
detailed structure and function. Further, the terms and phrases used herein are not
intended to be limiting, but rather, to provide an understandable description of the
concepts.
[0023] The terms "a" or "an", as used herein, are defined as one or more than one. The term
plurality, as used herein, is defined as two or more than two. The term another, as
used herein, is defined as at least a second or more. The terms "including" and "having,"
as used herein, are defined as comprising (i.e., open language).
[0024] With reference to FIGS. 1-3, the disclosure provides an expandable spacer 100 having
an adjustable height. The implant is inserted between two adjacent bony surfaces to
facilitate separation of the bones, and if desired, can promote the fusion of the
bony surfaces. Although intended to be useful with any adjacent bony surface in which
fusion is desired, the implant is advantageously applied to insertion between two
adjacent vertebral bodies in any section of the spine, including the cervical, thoracic,
lumbar, and sacral vertebral sections. More than one spacer 100 may be implanted within
the body, for example between successive or separated vertebrae, between adjacent
vertebrae. The use of multiple implants is particularly advantageous for patients
whose back pain is not limited to a localized area, or for patients whose localized
damage has progressed to other areas of the spine.
[0025] The implant and methods for its insertion can be used in a treatment protocol for
any of a wide variety of conditions in a patient involving diseased or damaged bony
structures. The patient can be a human being. Additionally, it is contemplated that
the implant may be useful in veterinary science for any animal having adjacent bony
structures to be fused. The implant can collapse, for example, to approximately one
half of an expanded size. When in this collapsed configuration, the implant can be
inserted into a space through a small incision and narrow pathways, using appropriate
minimally-invasive techniques, and can be positioned within the space between adjacent
bones, and there expanded to a desired therapeutic height. The incision may be short,
for example about one inch in length, which is smaller than the implant in an expanded
configuration. If the desired position and/or expansion are not achieved, the implant
can be collapsed, repositioned, and re-expanded in situ.
[0026] Although the implant is exemplified herein for use in the spine, the implant is contemplated
for fusion of any bony structures. While the implants are described herein using several
varying embodiments, the implants are not limited to these embodiments. An element
of one embodiment may be used in another embodiment, or an embodiment may not include
all described elements.
[0027] With reference to FIGS. 1-5, a spacer 100 of the disclosure includes endplates 102,
104 having expansion ramps 150, mateable with moveable lift ramps 250 of a carriage
200. In the embodiment shown, endplates 102, 104 are symmetrical, and spacer 100 can
be implanted with either endplate positioned superior with respect to the other. In
other embodiments, they may be dissimilar, and a particular orientation may then be
advantageous or necessary.
[0028] Spacer 100 forms a distal end 154 which is inserted first into the body, and which
can be tapered to facilitate insertion between body tissue, and a proximal end 156,
to which a tool may be connected. Distal and proximal ends 154 and 156 define a longitudinal
plane 158, extending therebetween. To expand Spacer 100, lift ramps 250 are displaced
relative to endplates 102, 104, causing expansion ramps 150 to slide along lift ramps
250, thereby moving endplates 102, 104 relatively apart, thereby increasing a height
of Spacer 100. Body tissue engaging projections 152, for example tooth shaped projections,
can be provided upon a surface of endplate 102, 104, to further secure spacer 100
in a therapeutic location.
[0029] Lift ramps 250 extend from carriage 200, which is slideably retained within a frame
126 extending between endplates 102, 104. Carriage 200 is displaced relative to endplates
102, 104 by being pulled by a pin 106 connected to a link 108 threadably connected
to an actuating screw 110. One or more guide elements 112, associated with frame 126,
can be provided to prevent endplates 102, 104 from moving along longitudinal axis
158 along with carriage 200, thereby causing lift ramps 250 and expansion ramps 150
to be moved relative to each other, expanding or contracting Spacer 100. Actuating
screw can be prevented from moving along longitudinal axis by a blocking flange 114
or 174.
[0030] With further reference to FIGS. 6-7, in accordance with the disclosure, an articulating
screw support 160 is slideably retained in connection with frame 126 by, in one embodiment,
a flanged connection 162. In this manner, a longitudinal axis 168, defined by screw
support 160 and pin 106, may form a changeable angle (α) with respect to longitudinal
axis 158 of endplates 102, 104, or a longitudinal axis of frame 126. Actuating screw
110 is rotatably confined within screw support 160, and is threadably engaged with
link 108. Pin 106 pivotally retains link 108 in connection with carriage 200. A slot
202, associated with carriage 200, enables movement of pin 106, whereby pin 106 and
link 108 can maintain a fixed orientation with respect to screw support 160, regardless
of an angular disposition of screw support 160. Slot 202 is thus configured and dimensioned
to enable a location of pin 106, confined therewithin, to correspond to a path of
travel of screw support 160 as defined by connection 162.
[0031] In one embodiment, a path of travel of screw support 160 is defined by connection
162 to maintain a fixed orientation of carriage 200 with respect to frame 126. More
particularly, if screw support 160 is moved along a path which does not pivot about
a single point defined by a current location of pin 106, pin 106 may move within slot
202 to maintain a fixed distance in a contracted position between pin 106 and screw
support 160, and therefore carriage 200 is not caused to be moved as screw support
160 is moved. In other embodiments, slot 202 is defined to cause a predetermined movement
of carriage 200 as screw support 160 is moved.
[0032] Similarly, regardless of a given orientation of screw support 160, rotation of actuating
screw advances or retards link 108 and pin 106, causing movement of carriage 200 relative
to endplates 102, 104. More particularly, slot 202 defines a longitudinal axis 268,
which is oriented to lie at a non-perpendicular angle (β) with respect to longitudinal
axis 168 of screw support 160, through a substantial portion of the range of motion
of screw support 160. In this manner, once a desired orientation of screw support
160 has been established, rotation of actuating screw 110 causes pin 106 to push or
pull along an edge of slot 202, thereby causing movement of carriage 200. If axis
168 and 268 are perfectly perpendicular, it is possible no movement can be caused
by threading screw 110; however, as a practical matter, reorienting screw support
160 a very small amount can resolve this theoretical limitation. Carriage 200 is slideably
retained by a channel or edge interface 116 formed between carriage 200 and at least
one endplate 102, 104, thereby limiting movement of carriage 200 along longitudinal
axis 158.
[0033] With reference to FIGS. 8-15, an alternative spacer 100A of the disclosure functions
in analogous manner to the embodiment of FIGS. 1-7, however in this embodiment, rotation
of actuating screw 110A causes carriage 200A to push endplates 102A, 104A to cause
expansion. More particularly, an orientation of expansion ramps 150A and lift ramps
250A are oriented 180 degrees with respect to longitudinal axis 158. The embodiment
of FIGS. 8-9 additionally illustrates an alternative actuating screw 110A configuration,
in which screw 110A is rotatably connected to link 108A, and threadably connected
within screw support 160A, whereby screw 110A moves along longitudinal axis 168 within
a threaded bore 118A of screw support 160A. Screw 110A causes movement of link 108A,
which advances or retards pin 106 within slot 202, to cause a corresponding movement
of carriage 200A. As the various aspects of differing embodiments of the disclosure
may be substituted where logical, generally, it may be seen that this alternative
screw 110A configuration can be used with other embodiments of the disclosure, as
well.
[0034] As may be seen in FIG. 2, for example, in one embodiment, connection 162 includes
interlocking mating flanges 164, 166, associated with frame 126 and screw support
160, respectively. Flanges 164, 166 form mutually curved guide surfaces defining a
path of movement for screw support 160 relative to frame 126, and retain screw support
160 in engagement with frame 126. Other configurations are possible, provided screw
support 160 and frame 126 may form different angular dispositions with respect to
each other, and wherein actuating screw 110 or 110A (FIG. 8) may interact with carriage
200 or 200A to slide carriage 200 or 200A with respect to frame 126, 126A.
[0035] Turning now to FIGS. 16-18, spacer 100B includes curved endplates 102B, 104B, and
a curved carriage 200B slideable within edge interface 116B. Carriage 200B includes
a threaded bore 218, into which actuating screw 110B is threaded. As screw 110B is
rotated in a first direction, carriage 200B is moved towards distal end 154, and as
screw 110B is rotated in a second, opposite direction, carriage 200B is moved away
from distal end 154. Depending upon the angular direction of ramps 150E and 250B,
endplates 102B, 104B are moved together or apart, as described with respect to the
embodiments of FIGS. 1 and 8. Spacer 100E forms, overall, a curved shape, which can
advantageously be rotated as it is inserted through a minimal incision, to thereby
become implanted between adjacent bones. This reduces an extent of a requirement of
rotating a spacer, within the body, prior to insertion between the bones, thus reducing
an adverse impact to adjacent body tissue.
[0036] As actuating screw 110B threads into carriage 200B, shaft 140 and head 142 of screw
110B are angularly displaced with respect to screw support 160B. Accordingly, screw
support 160B is provided with a gapped region 170, allowing movement of screw 110B.
Additionally, screw support 160B is retained in connection with a frame 126B by a
flanged connection 162B, in this case a dovetail connection. Connection 162B enables
screw support 160B to be angled with respect to frame 126B, to facilitate access to
screw 110B by a tool (not shown), when spacer 100B is implanted within the body, and
to further enable screw 110B to change an angle with respect to frame 126B.
[0037] Frame 126B is connected to each of endplates 102B, 104B by a flanged connector, in
this embodiment a dovetail formed between endplate flanges 178 extending from each
of endplates 102B, 104B, and frame flanges 180 associated with an intermediate connector
182. Actuating screw 110B can be rotatably retained within screw support 160B by a
washer or flange (not shown) positioned in groove 186 within screw support 160B, or
intermediate connector 182 can be configured to rotatably retain screw 100B.
[0038] With reference to FIGS. 16-21, a spacer 100C functions in a similar manner to spacers
100, 100A, and 100B, with the following distinctions. Initially, in the embodiment
shown, screw support 160C does not slide along a flanged connector 162, and is connected
to endplates 102C, 104C in a like manner as spacer 100B. However, screw support 160C
could be connected to a remainder of spacer 100C using a flange connector 162. Additionally,
actuating screw 110C has a tool engagement 188C that is different than the tool engagement
of other embodiments, although engagement style 188, or any other style tool engagement,
may be provided upon screw 110C. Engagement stylet 188 allows for articulating between
the holder and the implant by pivot point 192.
[0039] As may best be seen in FIG. 20, 21, nut 198 retains actuating screw 110C in connection
with carriage 200C. However, in distinction with respect to threaded bore 218 of spacer
100B, nut 198 may toggle, or change an angular orientation with respect to carriage
200C, as screw 100C is rotated, and carriage 200C is moved. Nut 198 can be provided
with a nut bearing surface 198', which mateably interacts with a carriage bearing
surface 208. Similar bearing surfaces 198" and 208' can be provided on an opposite
side of nut 198, for pushing carriage 200C in an opposite direction. In the embodiment
shown, threading nut 198 in the direction of proximal end 156 causes an expansion
or increase in height of spacer 100C, and threading nut 198 in a direction of distal
end 154 causes a reduction, or decrease in height of spacer 100C. However, ramps 150C
and 250C can be oriented to cause an opposite effect.
[0040] The following discussion pertains to all embodiments of the disclosure, including
spacers 100, 100A, 100B, and 100C. For brevity, the letter suffix designating variations
of like parts will be omitted, unless a specific distinction is made. For all spacer
100 embodiments of the disclosure, carriage 200 can be slid, or actuated, when screw
support 60 is disposed at an angle with respect to the carriage. In the embodiments
of FIGS. 1-15, this angle may vary between 0° and 70°, and with modifications, this
angle could be increased to a theoretical maximum approaching 180°. The embodiment
of FIGS. 16-18 accomplishes disposing screw 100B at an angle to the endplate bodies
by curving the endplates, and by configuring bore 218 at an angle with respect to
carriage 200B.
[0041] In all embodiments, head 142 of screw 110 may be accessed by a driving tool extending
from outside the body, into the body, while endplates 102, 104 lie at an angle, for
example perpendicular, to a pathway into the body. More particularly, spacers 100
of the disclosure may be inserted between vertebral bodies when in a collapsed or
non-expanded state, from any approach to the spine. As spacer 100 is inserted between
endplates, it is rotated to contact cortical bone of the endplates, and to avoid anatomical
structures which should not be disturbed.
[0042] Once rotated into position, screw support 160 can be turned towards an exterior of
the body, if it has not already been so turned, whereby a tool may be conveniently
mated with a tool engagement 188 of screw head 142. After screw 110 is rotated, endplates
102, 104 separate, expanding or increasing a height of spacer 100, and restoring and
maintaining a therapeutic spacing between adjacent bones. In some embodiments, after
expansion of spacer 100, screw support 160 may slide along flanged connection 162
to lie at an optimal orientation with respect to body tissue, for example 0 degrees
with respect to carriage 200, or at an angle deemed best by the medical practitioner.
[0043] Spacers 100 may include ramps 150, 250 of differing height within a spacer, whereby
endplates 102, 104 mutually separate at different rates at distal and proximal ends
154, 156, or at sides transverse to distal and proximal ends 154, 156, whereby an
angular disposition of adjacent bones may be changed, for example to correct lordosis
or scoliosis. Endplates 102, 104 may additionally, or alternatively, be resilient,
so that they may conform to bony surfaces, forming a more stable support platform.
Accordingly, endplates 102, 104 can be fabricated from a polymeric material, a naturally
resilient material, or a resilient metal, for example a shape memory alloy, or any
other resilient biocompatible material of sufficient strength and durability for separating
bones within the body. Spacers 100 may further be removed or repositioned during an
initial implantation procedure, or later in time.
[0044] In accordance with the disclosure, during implantation of intervertebral spacers
from a posterior approach, there is a need to avoid damaging nerve roots. A prior
art spacer dimensioned to separate bones can block a view of nerve roots as it is
inserted, and due to its large size, poses a greater risk of contacting nerve roots
during insertion into the body. As a result, the medical practitioner must more often
retract nerve roots, with attendant danger of tissue damage. Spacers 100 of the disclosure
form a smaller dimension during implantation, relative to a final dimension for spacing
bones. Accordingly, nerve roots can be visualized and avoided during insertion, and
nerve root manipulation can be avoided or minimized.
[0045] As spacers 100 of the disclosure can be articulated during implantation, they can
be inserted between bones by being passed through a minimally invasive entry, for
example through an incision approximating the smallest collapsed dimension, for example
transverse to a longitudinal dimension extending between distal and proximal ends
154, 156. This enables exceptional anterior placement without impaction, as well as
facilitating implantation from other approaches. Implants of the disclosure further
develop a good bone contact area, as an implant with a larger footprint may be inserted
through a reduced size incision, due to the overall dimensions of the implant being
reduced during insertion.
[0046] Spacers 100 of the disclosure enable a continuous expansion and retraction over a
range of displacements according to predetermined dimensions of a specific spacer
design. This provides the ability to distract vertebral bodies or other bones to a
desired height or separation. Endplates 102, 104 can be shaped to form planes or surfaces
which converge relative to each, to provide for proper lordosis, and can be provided
with openings 190 through which bone may grow, and into which bone graft material
may be placed. Spacers 100 of the disclosure may be used to distract, or force bones
of a joint apart, or may be used to maintain a separation of bones created by other
means, for example by a retractor. Endplates may additionally be curved to conform
to the surface of body tissue, for example the surface of cortical bone, of the vertebra
to be contacted, for improved fixation and load bearing.
[0047] Spacers 100 of the disclosure may be further secured in connection with the body
by passage of elongated fasteners through frame 162, or an endplate 102, 104. As described
therein, a blocking mechanism can be used to prevent backing out of the elongated
fastener. Similarly, screw 110 can be provided with a blocking mechanism as described
in the foregoing reference, or a resilient washer (not shown) may be positioned within
groove 186, to resist unintended rotation of screw 110.
[0048] Implants of the disclosure may be fabricated using any biocompatible materials known
or hereinafter discovered, having sufficient strength, flexibility, resiliency, and
durability for the patient, and for the term during which the device is to be implanted.
Examples include but are not limited to metal, such as, for example titanium and chromium
alloys; polymers, including for example, PEEK or high molecular weight polyethylene
(HMWPE); and ceramics. There are many other biocompatible materials which may be used,
including other plastics and metals, as well as fabrication using living or preserved
tissue, including autograft, allograft, and xenograft material.
[0049] Portions or all of the implant may be radiopaque or radiolucent, or materials having
such properties may be added or incorporated into the implant to improve imaging of
the device during and after implantation.
[0050] Spacers 100 may be formed using titanium, or a cobalt-chrome-molybdenum alloy, Co-Cr-Mo,
for example as specified in ASTM F1537 (and ISO 5832-12). The smooth surfaces may
be plasma sprayed with commercially pure titanium, as specified in ASTM F1580, F1978,
F1147 and C-633 (and ISO 5832-2). Alternatively, part or all of spacers 100 may be
formed with a polymer, for example ultra-high molecular weight polyethylene, UHMWPE,
for example as specified in ASTM F648 (and ISO 5834-2). In one embodiment, PEEK-OPTIMA
(a trademark of Invibio Ltd Corp, United Kingdom) may be used for one or more components
of the implants of the disclosure. For example, polymeric portions can be formed with
PEEK-OPTIMA, which is radiolucent, whereby bony ingrowth may be observed. Other polymeric
materials with suitable flexibility, durability, and biocompatibility may also be
used.
[0051] In accordance with the invention, implants of various sizes may be provided to best
fit the anatomy of the patient. Components of matching or divergent sizes may be assembled
during the implantation procedure by a medical practitioner as best meets the therapeutic
needs of the patient, the assembly inserted within the body using an insertion tool.
Implants of the invention may also be provided with an overall angular geometry, for
example an angular mating disposition of endplates, to provide for a natural lordosis,
or a corrective lordosis, for example of from 0° to 12° for a cervical application,
although much different values may be advantageous for other joints. Lordotic angles
may also be formed by shaping one or both endplates to have relatively non-coplanar
surfaces.
[0052] Expanded implant heights, for use in the cervical vertebrae for example, may typically
range from 7 mm to 12 mm, but may be larger or smaller, including as small as 5 mm,
and as large as 16 mm, although the size is dependent on the patient, and the joint
into which an implant of the invention is to be implanted. Spacers 100 may be implanted
within any level of the spine, and may also be implanted in other joints of the body,
including joints of the hand, wrist, elbow, shoulder, hip, knee, ankle, or foot.
[0053] In accordance with the invention, a single spacer 100 may be used, to provide stabilization
for a weakened joint or joint portion. Alternatively, a combination of two, three,
or more of any of spacer 100 may be used, at a single joint level, or in multiple
joints. Moreover, implants of the disclosure may be combined with other stabilizing
means.
[0054] Additionally, spacers 100 of the disclosure may be fabricated using material that
biodegrades in the body during a therapeutically advantageous time interval, for example
after sufficient bone ingrowth has taken place. Further, implants of the disclosure
are advantageously provided with smooth and or rounded exterior surfaces, which reduce
a potential for deleterious mechanical effects on neighboring tissues.
[0055] Any surface or component of an implant of the disclosure may be coated with or impregnated
with therapeutic agents, including bone growth, healing, antimicrobial, or drug materials,
which may be released at a therapeutic rate, using methods known to those skilled
in the art.
[0056] Devices of the disclosure provide for adjacent vertebrae to be supported during flexion/extension,
lateral bending, and axial rotation. In one embodiment, spacer 100 is indicated for
spinal arthroplasty in treating skeletally mature patients with degenerative disc
disease, primary or recurrent disc herniation, spinal stenosis, or spondylosis in
the lumbosacral spine (LI-SI). Degenerative disc disease is advantageously defined
as discogenic back pain with degeneration of the disc confirmed by patient history
and radiographic studies, with or without leg (radicular) pain. Patients are advantageously
treated, for example, who may have spondylolisthesis up to Grade 1 at the involved
level. The surgery position spacer 100 may be performed through an Anterior, Anterolateral,
Posterolateral, lateral or any approach.
[0057] In a typical embodiment, spacer implants of the disclosure have an uncompressed height,
before insertion, of 7 to 13mm, and may advantageously be provided in cross-sections
of 10×27mm, 12×32mm and 12×37mm, with 4, 8, 12, or 16 degree lordotic angles, although
these are only representative sizes, and substantially smaller or larger sizes can
be therapeutically beneficial. In one embodiment implants in accordance with the instant
disclosure are sized to be inserted using an MIS approach, for example using a reduced
incision size, for example less than about 5 cm, and advantageously less than about
2.5 cm, with fewer and shorter cuts through body tissue. Spacer 100 may advantageously
be used in combination with other known or hereinafter developed forms of stabilization
or fixation, including for example rods and plates.
[0058] Spacer implants of the disclosure can be inserted into the body, advantageously in
a contracted or non-expanded configuration, through a transforaminal approach, and
can articulate in attachment to an inserter tool (not shown), for example for anterior
placement. Once placement is achieved, the implant is capable of expanding for disc
height restoration. To maintain an engagement spacer 100 and an insertion tool, a
driving end (not shown) of the tool is inserted into tool engagement 188. To prevent
separation of the tool and spacer 100, a tool connector 192 may be provided, extending
from or formed within screw support 60. In the embodiment shown in FIG. 16, for example,
tool connector 192 extends from a surface of screw support 60B, and is releaseably
grasped by a mating tool portion.
[0059] Portions of spacer 100 may be radiopaque or radiotransparent. To improve visibility
under imaging, radiopaque elements 194 may be provided in predetermined locations
within spacer 100. In the embodiment of FIG. 16, for example, elements 194 are positioned
within at least one of endplate 102B, 104B.
[0060] Implant spacers 100 of the disclosure can be positioned anterioriorly and continuously
expanded to provide axial balance and greater endplate contact area, and allow for
superior sagittal correction, and are insertable into the body through a smaller window,
decreasing the need for damage and trauma to body tissue. Spacers 100 of disclosure
provide the benefits of an ALIF device, implantable through a familiar posterior approach,
decreasing surgery time and associated blood loss, as well as eliminating the need
for an access surgeon.
1. Abstandshalter (100) zum Trennen von Knochen eines Gelenks, wobei der Abstandshalter
umfasst:
einen Rahmen (126);
einen Schlitten (200), der relativ zum Rahmen (126) verschiebbar beweglich ist und
zumindest eine Rampenfläche aufweist;
eine Betätigungsschraube (110), die mit dem Schlitten verbunden ist und vom Rahmen
abgestützt wird, wobei die Betätigungsschraube (110) dazu konfiguriert ist, zu bewirken,
dass sich der Schlitten relativ zum Rahmen (126) verschiebbar bewegt, wenn die Betätigungsschraube
(110) gedreht wird;
eine erste Endplatte (102), die zum Eingriff mit einem ersten Knochen des Gelenks
konfiguriert ist und die zumindest eine Rampenfläche (150) aufweist, die mit der zumindest
einen Schlitten-Rampenfläche (250) zusammenpassbar ist, wobei, wenn der Schlitten
(200) durch Drehen der Betätigungsschraube (110) verschiebbar bewegt wird, die zumindest
eine Endplatten-Rampenfläche (150) sich gegen die zumindest eine Schlitten-Rampenfläche
(250) verschiebt, um zu bewirken, dass sich die erste Endplatte (102) entlang einer
Achse quer zu einer Längsachse bewegt, um eine Höhe des Abstandshalters (100) zu vergrößern;
eine zweite Endplatte (104), die zum Eingriff mit einem zweiten Knochen des Gelenks
konfiguriert ist, dadurch gekennzeichnet, dass der Abstandshalter (100) ferner umfasst:
einen Schraubenträger (160), der mit dem Rahmen (126) verbunden ist und zum drehbaren
Halten der Betätigungsschraube (110) konfiguriert ist, wobei der Schraubenträger (160)
eine Längsachse bildet und der Rahmen eine Längsachse bildet, wobei der Schraubenträger
(160) mit dem Rahmen (126) verschiebbar verbunden ist, um eine Änderung einer Winkelausrichtung
zwischen der Betätigungsschraube (110) und dem Rahmen (126) zu ermöglichen, wobei
der Abstandshalter ferner umfasst:
einen Stift (106), der im Innern eines im Schlitten (200) ausgebildeten Schlitzes
beweglich ist; und
ein Verbindungselement (108), das am Stift (106) schwenkbar befestigt ist und eine
Gewindebohrung aufweist, in welche die Betätigungsschraube (110) einschraubbar ist,
um eine verschiebbare Bewegung des Schlittens (200) im Innern des Rahmens (126) zu
bewirken.
2. Abstandshalter nach Anspruch 1, wobei die erste oder zweite Endplatte (102, 104) entlang
ihrer Länge kontinuierlich gekrümmt ist.
3. Abstandshalter nach Anspruch 1, wobei die Betätigungsschraube (110) durch eine Mutter
(198) am Schlitten (200) befestigt ist.
4. Abstandshalter nach Anspruch 3, wobei die Mutter (198) und der Schlitten (200) dazwischen
eine zusammenpassende gekrümmte Lagerfläche bilden.
5. Abstandshalter nach Anspruch 1, wobei der Schraubenträger (160) mit dem Rahmen (126)
durch eine Flanschverbindung (162) verschiebbar verbunden ist.
6. Abstandhalter nach Anspruch 1, wobei die erste Endplatte (102) mit dem Rahmen (126)
durch eine verschiebbare Flanschverbindung verbunden ist.
7. Abstandhalter nach Anspruch 1, wobei die zweite Endplatte (104) durch eine Flanschverbindung
verschiebbar in Verbindung mit dem Rahmen (126) gehalten wird.
8. Abstandhalter nach Anspruch 1, wobei der Schraubenträger (160) mit dem Rahmen (126)
schwenkbar verbunden ist und die Betätigungsschraube (110) drehbar abstützt.
9. Abstandshalter nach Anspruch 1, wobei der Schlitten (200) zumindest zwei Rampenflächen
(250) umfasst und die zweite Endplatte (104) zumindest eine Rampenfläche umfasst,
die mit zumindest einer der zumindest zwei Rampenflächen (250) des Schlittens (200)
zusammenpassbar ist, wobei, wenn der Schlitten (200) durch Drehen der Betätigungsschraube
(110) verschiebbar bewegt wird, die zumindest eine zweite Endplatten-Rampenfläche
sich gegen die zumindest eine zusätzliche Schlitten-Rampenfläche verschiebt, um zu
bewirken, dass sich die zweite Endplatte (104) entlang einer Achse quer zur Längsachse
bewegt, um eine Höhe des Abstandshalters (100) zu vergrößern.
10. Abstandshalter nach Anspruch 1, wobei die erste Endplatte (102) so konfiguriert ist,
dass diese am Rahmen (126) anliegt, wenn die erste Endplatte (102) entlang einer Achse
quer zur Längsachse bewegt wird, wobei sich die erste Endplatte (102) im Wesentlichen
nur entlang einer Achse quer zur Längsachse bewegt.
11. Abstandshalter nach Anspruch 1, wobei die erste Endplatte (102) und/oder der Rahmen
(126) zumindest eine Öffnung umfasst, durch die ein Befestigungselement hindurchgeführt
werden kann, um den Abstandshalter (100) an einem Knochen des Gelenks zu befestigen.
12. Abstandshalter nach Anspruch 1, wobei die erste Endplatte (102) einen oder mehrere
Vorsprünge (152) umfasst, die zum Eingriff mit dem Knochen des Gelenks konfiguriert
sind, wenn der Abstandshalter (100) zwischen Knochen des Gelenks positioniert ist.